Spindle cell variant of ameloblastic carcinoma: a case report and review of literature

Ameloblastic carcinoma is a rare and malignant odontogenic tumor. Approximately, 100 cases of ameloblastic carcinomas have been reported in the literature, with fewer than 10 reported cases of an even more rare variant with spindle-cell differentiation. Although it is presumed that most ameloblastic...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Military medicine 2015-05, Vol.180 (5), p.e614-e617
Hauptverfasser: McNaught, Michael J, Turella, Stephen J, Fallah, David M, Demsar, William J
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e617
container_issue 5
container_start_page e614
container_title Military medicine
container_volume 180
creator McNaught, Michael J
Turella, Stephen J
Fallah, David M
Demsar, William J
description Ameloblastic carcinoma is a rare and malignant odontogenic tumor. Approximately, 100 cases of ameloblastic carcinomas have been reported in the literature, with fewer than 10 reported cases of an even more rare variant with spindle-cell differentiation. Although it is presumed that most ameloblastic carcinomas arise de novo, it also appears capable of proliferating as carcinoma ex ameloblastoma. Without a full past history, the exact origin of these tumors can be unclear. The exact classification becomes further questionable when both an intraosseous and peripheral tumor exists. This currently reported case has been present for at least 4 years before the patient presenting for care. However, without prior biopsy, the etiology and category of this ameloblastic carcinoma is speculative. Our case represents a histologically unequivocal case of ameloblastic carcinoma. Based on tumor morphology, questions still remain, as to whether it arose de novo, or as carcinoma ex ameloblastoma. The possibility of categorizing the current lesion as a spindle cell variant also exists because of the presence of a prominent population of malignant epithelial spindled cells arranged in fascicles. The authors believe that this ameloblastic carcinoma would best be subclassified as a rare spindle cell variant, based on the prominent spindle cell component.
doi_str_mv 10.7205/MILMED-D-14-00509
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1680182180</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1680182180</sourcerecordid><originalsourceid>FETCH-LOGICAL-c372t-75cb82dc3df833067ddee7d27297d7f973bdf8bf60e8624c476af81d14ad10df3</originalsourceid><addsrcrecordid>eNpdkMtOwzAQRS0EoqXwAWyQJTZsAuNHYocdagtUasWCh9hZju1IqfLCTor4e1JaWLCaGc25ozsXoXMC14JCfLNaLFfzWTSLCI8AYkgP0JikDKKEsPdDNAagScRBxCN0EsIagPBUkmM0onHKUkLpGL09t0VtS4eNK0u80b7QdYebHOvKlU1W6tAVBhvtTVE3lb7FehiCw961je-wru3Qbgr3udWURee87nrvTtFRrsvgzvZ1gl7v5y_Tx2j59LCY3i0jwwTtIhGbTFJrmM0lY5AIa50TlgqaCivyVLBs2GR5Ak4mlBsuEp1LYgnXloDN2QRd7e62vvnoXehUVYTtK7p2TR8USSQQSYmEAb38h66b3teDu4ESqRScDR4miOwo45sQvMtV64tK-y9FQG1DV7vQ1UwRrn5CHzQX-8t9Vjn7p_hNmX0DGF59aQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1679874383</pqid></control><display><type>article</type><title>Spindle cell variant of ameloblastic carcinoma: a case report and review of literature</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>McNaught, Michael J ; Turella, Stephen J ; Fallah, David M ; Demsar, William J</creator><creatorcontrib>McNaught, Michael J ; Turella, Stephen J ; Fallah, David M ; Demsar, William J</creatorcontrib><description>Ameloblastic carcinoma is a rare and malignant odontogenic tumor. Approximately, 100 cases of ameloblastic carcinomas have been reported in the literature, with fewer than 10 reported cases of an even more rare variant with spindle-cell differentiation. Although it is presumed that most ameloblastic carcinomas arise de novo, it also appears capable of proliferating as carcinoma ex ameloblastoma. Without a full past history, the exact origin of these tumors can be unclear. The exact classification becomes further questionable when both an intraosseous and peripheral tumor exists. This currently reported case has been present for at least 4 years before the patient presenting for care. However, without prior biopsy, the etiology and category of this ameloblastic carcinoma is speculative. Our case represents a histologically unequivocal case of ameloblastic carcinoma. Based on tumor morphology, questions still remain, as to whether it arose de novo, or as carcinoma ex ameloblastoma. The possibility of categorizing the current lesion as a spindle cell variant also exists because of the presence of a prominent population of malignant epithelial spindled cells arranged in fascicles. The authors believe that this ameloblastic carcinoma would best be subclassified as a rare spindle cell variant, based on the prominent spindle cell component.</description><identifier>ISSN: 0026-4075</identifier><identifier>EISSN: 1930-613X</identifier><identifier>DOI: 10.7205/MILMED-D-14-00509</identifier><identifier>PMID: 25939122</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Ameloblastoma - pathology ; Carcinoma - pathology ; Humans ; Male ; Mandibular Neoplasms - pathology ; Middle Aged</subject><ispartof>Military medicine, 2015-05, Vol.180 (5), p.e614-e617</ispartof><rights>Reprint &amp; Copyright © 2015 Association of Military Surgeons of the U.S.</rights><rights>Copyright Association of Military Surgeons of the United States May 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-75cb82dc3df833067ddee7d27297d7f973bdf8bf60e8624c476af81d14ad10df3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25939122$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McNaught, Michael J</creatorcontrib><creatorcontrib>Turella, Stephen J</creatorcontrib><creatorcontrib>Fallah, David M</creatorcontrib><creatorcontrib>Demsar, William J</creatorcontrib><title>Spindle cell variant of ameloblastic carcinoma: a case report and review of literature</title><title>Military medicine</title><addtitle>Mil Med</addtitle><description>Ameloblastic carcinoma is a rare and malignant odontogenic tumor. Approximately, 100 cases of ameloblastic carcinomas have been reported in the literature, with fewer than 10 reported cases of an even more rare variant with spindle-cell differentiation. Although it is presumed that most ameloblastic carcinomas arise de novo, it also appears capable of proliferating as carcinoma ex ameloblastoma. Without a full past history, the exact origin of these tumors can be unclear. The exact classification becomes further questionable when both an intraosseous and peripheral tumor exists. This currently reported case has been present for at least 4 years before the patient presenting for care. However, without prior biopsy, the etiology and category of this ameloblastic carcinoma is speculative. Our case represents a histologically unequivocal case of ameloblastic carcinoma. Based on tumor morphology, questions still remain, as to whether it arose de novo, or as carcinoma ex ameloblastoma. The possibility of categorizing the current lesion as a spindle cell variant also exists because of the presence of a prominent population of malignant epithelial spindled cells arranged in fascicles. The authors believe that this ameloblastic carcinoma would best be subclassified as a rare spindle cell variant, based on the prominent spindle cell component.</description><subject>Ameloblastoma - pathology</subject><subject>Carcinoma - pathology</subject><subject>Humans</subject><subject>Male</subject><subject>Mandibular Neoplasms - pathology</subject><subject>Middle Aged</subject><issn>0026-4075</issn><issn>1930-613X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkMtOwzAQRS0EoqXwAWyQJTZsAuNHYocdagtUasWCh9hZju1IqfLCTor4e1JaWLCaGc25ozsXoXMC14JCfLNaLFfzWTSLCI8AYkgP0JikDKKEsPdDNAagScRBxCN0EsIagPBUkmM0onHKUkLpGL09t0VtS4eNK0u80b7QdYebHOvKlU1W6tAVBhvtTVE3lb7FehiCw961je-wru3Qbgr3udWURee87nrvTtFRrsvgzvZ1gl7v5y_Tx2j59LCY3i0jwwTtIhGbTFJrmM0lY5AIa50TlgqaCivyVLBs2GR5Ak4mlBsuEp1LYgnXloDN2QRd7e62vvnoXehUVYTtK7p2TR8USSQQSYmEAb38h66b3teDu4ESqRScDR4miOwo45sQvMtV64tK-y9FQG1DV7vQ1UwRrn5CHzQX-8t9Vjn7p_hNmX0DGF59aQ</recordid><startdate>201505</startdate><enddate>201505</enddate><creator>McNaught, Michael J</creator><creator>Turella, Stephen J</creator><creator>Fallah, David M</creator><creator>Demsar, William J</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88F</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M1Q</scope><scope>M2M</scope><scope>M2P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>201505</creationdate><title>Spindle cell variant of ameloblastic carcinoma: a case report and review of literature</title><author>McNaught, Michael J ; Turella, Stephen J ; Fallah, David M ; Demsar, William J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-75cb82dc3df833067ddee7d27297d7f973bdf8bf60e8624c476af81d14ad10df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Ameloblastoma - pathology</topic><topic>Carcinoma - pathology</topic><topic>Humans</topic><topic>Male</topic><topic>Mandibular Neoplasms - pathology</topic><topic>Middle Aged</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McNaught, Michael J</creatorcontrib><creatorcontrib>Turella, Stephen J</creatorcontrib><creatorcontrib>Fallah, David M</creatorcontrib><creatorcontrib>Demsar, William J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Military Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Military Database</collection><collection>ProQuest Psychology</collection><collection>Science Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Military medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McNaught, Michael J</au><au>Turella, Stephen J</au><au>Fallah, David M</au><au>Demsar, William J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spindle cell variant of ameloblastic carcinoma: a case report and review of literature</atitle><jtitle>Military medicine</jtitle><addtitle>Mil Med</addtitle><date>2015-05</date><risdate>2015</risdate><volume>180</volume><issue>5</issue><spage>e614</spage><epage>e617</epage><pages>e614-e617</pages><issn>0026-4075</issn><eissn>1930-613X</eissn><abstract>Ameloblastic carcinoma is a rare and malignant odontogenic tumor. Approximately, 100 cases of ameloblastic carcinomas have been reported in the literature, with fewer than 10 reported cases of an even more rare variant with spindle-cell differentiation. Although it is presumed that most ameloblastic carcinomas arise de novo, it also appears capable of proliferating as carcinoma ex ameloblastoma. Without a full past history, the exact origin of these tumors can be unclear. The exact classification becomes further questionable when both an intraosseous and peripheral tumor exists. This currently reported case has been present for at least 4 years before the patient presenting for care. However, without prior biopsy, the etiology and category of this ameloblastic carcinoma is speculative. Our case represents a histologically unequivocal case of ameloblastic carcinoma. Based on tumor morphology, questions still remain, as to whether it arose de novo, or as carcinoma ex ameloblastoma. The possibility of categorizing the current lesion as a spindle cell variant also exists because of the presence of a prominent population of malignant epithelial spindled cells arranged in fascicles. The authors believe that this ameloblastic carcinoma would best be subclassified as a rare spindle cell variant, based on the prominent spindle cell component.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>25939122</pmid><doi>10.7205/MILMED-D-14-00509</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0026-4075
ispartof Military medicine, 2015-05, Vol.180 (5), p.e614-e617
issn 0026-4075
1930-613X
language eng
recordid cdi_proquest_miscellaneous_1680182180
source Oxford University Press Journals All Titles (1996-Current); MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Ameloblastoma - pathology
Carcinoma - pathology
Humans
Male
Mandibular Neoplasms - pathology
Middle Aged
title Spindle cell variant of ameloblastic carcinoma: a case report and review of literature
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T09%3A08%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Spindle%20cell%20variant%20of%20ameloblastic%20carcinoma:%20a%20case%20report%20and%20review%20of%20literature&rft.jtitle=Military%20medicine&rft.au=McNaught,%20Michael%20J&rft.date=2015-05&rft.volume=180&rft.issue=5&rft.spage=e614&rft.epage=e617&rft.pages=e614-e617&rft.issn=0026-4075&rft.eissn=1930-613X&rft_id=info:doi/10.7205/MILMED-D-14-00509&rft_dat=%3Cproquest_cross%3E1680182180%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1679874383&rft_id=info:pmid/25939122&rfr_iscdi=true